Gene: [0Xp11/IP1] incontinentia pigmenti, type I (sporadic; X-arrangement-associated);
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HET |
Basing on the data (Sefiani-1988,1989) about teh linkage of IP locus with DNA markers on the distal end of the chr X long arm, the HGM and GEM catalogues register the second IP gene (GEM:0Xq2/IP2), which determines the familial form of the incontinentia pigmenti syndrome (male-lethal)." |
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REF |
LOC "de Grouchy J &: Ann Genet, 28, 86-89, 1985 LOC "Gilgenkrantz S &: Ann Genet, 28, 90-92, 1985 LOC "Hodgson SV &: Hum Genet, 71, 231-234, 1985 COM,FAG "Sefiani A &: Hum Genet, 80, 282-286, 1988 COM,FAG "see GEM:0Xq2/IP2 |
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KEY |
derm |
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CLA |
unknown, basic |
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LOC |
0X p11.21-.1 |
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MIM |
MIM: 308300 |
